Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:16990255 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Synonyms

Uniprot VAR_058459

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts.

Variant displays